UniProtKB/Swiss-Prot Q9UKX5 : Variant p.Leu524Arg
Integrin alpha-11
Gene: ITGA11
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Variant information
Variant position:
524
The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:
LB/B
The variants are classified into three categories: LP/P, LB/B and US.LP/P: likely pathogenic or pathogenic. LB/B: likely benign or benign. US: uncertain significance
Residue change:
From Leucine (L) to Arginine (R) at position 524 (L524R, p.Leu524Arg).
Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties:
Change from medium size and hydrophobic (L) to large size and basic (R)
The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:
-2
The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another: Lowest score: -4 (low probability of substitution).Highest score: 11 (high probability of substitution). More information can be found on the following page
Other resources:
Links to websites of interest for the variant.
Sequence information
Variant position:
524
The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:
1188
The length of the canonical sequence.
Location on the sequence:
MYFNEGRERGKVYVYELRQN
L FVYNGTLKDSHSYQNARFGS
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation:
The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human MYFNEGRERGKVYVYELRQNL FVYNGTLKDSHSYQNARFGS
Mouse MYFSEGRERGKVYVYNLRQNR FVYNGTLKDSHSYQNARFGS
Sequence annotation in neighborhood:
The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
Chain
23 – 1188
Integrin alpha-11
Topological domain
23 – 1141
Extracellular
Repeat
462 – 527
FG-GAP 5
Glycosylation
528 – 528
N-linked (GlcNAc...) asparagine
Literature citations
Cloning, sequence analysis, and chromosomal localization of the novel human integrin alpha11 subunit (ITGA11).
Lehnert K.; Ni J.; Leung E.; Gough S.M.; Weaver A.; Yao W.P.; Liu D.; Wang S.-X.; Morris C.M.; Krissansen G.W.;
Genomics 60:179-187(1999)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 2); VARIANTS ARG-524; LEU-972 AND ILE-1003;
cDNA cloning and chromosomal localization of human alpha(11) integrin. A collagen-binding, I domain-containing, beta(1)-associated integrin alpha-chain present in muscle tissues.
Velling T.; Kusche-Gullberg M.; Sejersen T.; Gullberg D.;
J. Biol. Chem. 274:25735-25742(1999)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); TISSUE SPECIFICITY; VARIANTS ARG-524 AND LEU-972;
Submission
Xu Y.Y.; Sun L.Z.; Wu Q.Y.; Liu Y.Q.; Liu B.; Zhao B.; Wang X.Y.; Song L.; Ye J.; Sheng H.; Gao Y.; Zhang C.L.; Zhang J.; Wei Y.J.; Sun Y.H.; Jiang Y.X.; Zhao X.W.; Liu S.; Liu L.S.; Ding J.F.; Gao R.L.; Qiang B.Q.; Yuan J.G.; Liew C.C.; Zhao M.S.; Hui R.T.;
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 317-1188 (ISOFORM 1); VARIANTS ARG-524 AND LEU-972;
Disclaimer:
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.